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Delmuno 2.5 Mg/2.5 Mg Prolonged Release Tablets Delmuno 5 Mg/5 Mg Prolonged Release Tablets

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Delmuno 2.5 Mg/2.5 Mg Prolonged Release Tablets Delmuno 5 Mg/5 Mg Prolonged Release Tablets 1 SUMMARY OF THE PRODUCT CHARACTERISTICS 1 NAME OF THE MEDICINAL PRODUCT Delmuno 2.5 mg/2.5 mg prolonged release tablets Delmuno 5 mg/5 mg prolonged release tablets 2 QUALITATIVE AND QUANTITATIVE COMPOSITION 2.5 mg/2.5 mg tablets: Each tablet contains 2.5 mg of felodipine and 2.5 mg of ramipril. Each tablet contains 52 mg lactose anhydrous. For the full list of excipients, see section 6.1 5 mg/5 mg tablets: Each tablet contains 5 mg of felodipine and 5 mg of ramipril. Each tablet contains 51.5 mg lactose anhydrous. For the full list of excipients, see section 6.1 3 PHARMACEUTICAL FORM 2.5 mg/2.5 mg tablets: Delmuno 2.5 mg/2.5 mg tablets are circular (diameter approx 9 mm), apricot coloured, biconvex and H engraved on one side and marked 2.5 on the other side. OD 5 mg/5 mg tablets : Delmuno 5 mg/5 mg tablets are circular (diameter approx 9 mm), reddish-brown coloured, biconvex H and engraved on one side and marked 5 on the other side. OE 4 CLINICAL PARTICULARS 4.1 Therapeutic indications Treatment of essential hypertension. Delmuno fixed dose combination is indicated in patients whose blood pressure is not adequately controlled on felodipine or ramipril alone. 4.2 Posology and method of administration Posology Use in adults, including older people: One tablet Delmuno 2.5 mg/2.5 mg or Delmuno 5 mg/5 mg once daily, The maximum dose is two tablets Delmuno 2.5 mg/2.5 mg or one tablet Delmuno 5 mg/5 mg once daily. Special populations Use in patients with impaired liver function: See sections 4.3 and 4.4. 2 Use in patients with impaired renal function or patients already on diuretic treatment: See sections 4.3 and 4.4. Individual dose titration with the components can be recommended and when clinically appropriate, direct change from monotherapy to the fixed combination may be considered. Paediatric population: Delmuno is not recommended for use in children due to a lack of data. Method of administration Delmuno tablets should be swallowed whole with a sufficient amount of liquid. The tablets must not be divided, crushed or chewed. The tablet can be administered without food or following a light meal not rich in fat or carbohydrate. 4.3 Contraindications hypersensitivity to felodipine (or other dihydropyridines) ramipril, other angiotensin converting enzyme (ACE) inhibitors or any of the excipients listed in section 6.1. history of angioedema. concomitant use with sacubitril/valsartan therapy (see sections 4.4 and 4.5). unstable haemodynamic conditions: cardiovascular shock, untreated heart failure, acute myocardial infarction, unstable angina pectoris, stroke. haemodynamically significant cardiac valvular obstruction. dynamic cardiac outflow obstruction. AV block II or III. severely impaired hepatic function. severely impaired renal function (creatinine clearance less than 20 ml/min) and in patients on dialysis. pregnancy. lactation. The concomitant use of Delmuno with aliskiren-containing products is contraindicated in patients with diabetes mellitus or renal impairment (GFR <60 ml/min/1.73 m2) (see sections 4.5 and 5.1). 4.4 Special warnings and precautions for use Angioedema Angioedema occurring during treatment with an ACE inhibitor necessitates immediate discontinuation of the medicinal product. Angioedema may involve the tongue, glottis or larynx and, if so, may necessitate emergency measures. Angioedema of the face, extremities, lips, tongue, glottis or larynx has been reported in patients treated with ACE inhibitors. Emergency therapy should be given including, but not necessarily limited to, immediate subcutaneous adrenalin solution 1:1000 (0.3 to 0.5 ml) or slow intravenous adrenalin 1 mg/ml (observe dilution instructions) with control of ECG and blood pressure. The patient should be hospitalised and observed for at least 12 to 24 hours and should not be discharged until complete resolution of symptoms has occurred. Intestinal angioedema has been reported in patients treated with ACE inhibitors. These patients presented with abdominal pain (with or without nausea or vomiting); in some cases there was no prior history of facial angioedema and C1-esterase levels were normal. The angioedema was diagnosed by procedures including abdominal CT scan or ultrasound, or at surgery, and symptoms resolved after 3 stopping the ACE inhibitor. Intestinal angioedema should be included in the differential diagnosis of patients on ACE inhibitors presenting with abdominal pain. Compared with non-black patients, a higher incidence of angioedema has been reported in black patients treated with ACE inhibitors. This risk of angioedema may be increased in patients taking concomitant medications which may cause angioedema such as mTOR (mammalian target of rapamycin) inhibitors (e.g. temsirolimus, everolimus, sirolimus), vildagliptin or neprilysin (NEP) inhibitors (such as racecadotril). The combination of ramipril with sacubitril/valsartan is contraindicated due to the increased risk of angioedema (see sections 4.3 and 4.5). Dual blockade of the renin-angiotensin-aldosterone system (RAAS) There is evidence that the concomitant use of ACE-inhibitors, angiotensin II receptor blockers or aliskiren increases the risk of hypotension, hyperkalaemia and decreased renal function (including acute renal failure). Dual blockade of RAAS through the combined use of ACE-inhibitors, angiotensin II receptor blockers or aliskiren is therefore not recommended (see sections 4.5 and 5.1). If dual blockade therapy is considered absolutely necessary, this should only occur under specialist supervision and subject to frequent close monitoring of renal function, electrolytes and blood pressure. ACE-inhibitors and angiotensin II receptor blockers should not be used concomitantly in patients with diabetic nephropathy. Renal function Renal function should be monitored, particularly in the initial weeks of treatment with ACE inhibitors. Caution should be observed in patients with an activated renin-angiotensin system. Patients with mild to moderately impaired renal function (creatinine clearance 20-60 ml/min) and patients already on diuretic treatment: For dosage see the respective monoproducts. Electrolyte Monitoring: Hyperkalaemia Hyperkalaemia has been observed in some patients treated with ACE inhibitors, including ramipril. Patients at risk for the development of hyperkalaemia include those with renal insufficiency, age (>70 years), uncontrolled diabetes mellitus, or those using potassium salts, potassium-retaining diuretics, or other active substances increasing potassium (e.g. heparin, trimethoprim and in fixed dose combination with sulfamethoxazole, tacrolimus, ciclosporin); or condition such as dehydration, acute cardiac decompensation, metabolic acidosis. If concomitant use of the above mentioned agents is deemed appropriate, regular monitoring of serum potassium is recommended (see section 4.5). Electrolyte Monitoring: Hyponatremia Syndrome of Inappropriate Anti-Diuretic Hormone secretion (SIADH) and subsequent hyponatremia has been observed in some patients treated with ramipril. It is recommended that serum sodium levels be monitored regularly in older people and in other patients at risk of hyponatremia. Proteinuria It may occur particularly in patients with existing renal function impairment or on relatively high doses of ACE inhibitors. Renovascular hypertension/renal artery stenosis There is an increased risk of severe hypotension and renal insufficiency when patients with renovascular hypertension and pre-existing bilateral renal artery stenosis or stenosis of the artery to a solitary kidney are treated with ACE inhibitors. Loss of renal function may occur with only mild changes in serum creatinine even in patients with unilateral renal artery stenosis. There is no experience regarding the administration of Delmuno in patients with a recent kidney transplantation. 4 Hepatic failure Rarely, ACE inhibitors have been associated with a syndrome that starts with cholestatic jaundice and progress to fulminant hepatic necrosis and (sometimes) death. The mechanism of this syndrome is not understood. Patients receiving ACE inhibitors who develop jaundice or marked elevations of hepatic enzymes should discontinue the ACE inhibitor and receive appropriate medical follow-up. Patients with mild to moderately impaired liver function: For dosage see respective monoproducts. Surgery/Anaesthesia Hypotension may occur in patients undergoing major surgery or during treatment with anaesthetic agents that are known to lower blood pressure. If hypotension occurs, it may be corrected by volume expansion. Aortic stenosis/Hypertrophic cardiomyopathy ACE inhibitors should be used with caution in patients with haemodynamically relevant left- ventricular or outflow impediment (e.g. stenosis of the aortic or mitral valve, obstructive cardiomyopathy). The initial phase of treatment requires special medical supervision. Symptomatic hypotension In some patients, symptomatic hypotension may be observed after the initial dose, mainly in patients with heart failure (with or without renal insufficiency) treated with high doses of loop diuretics, in hyponatraemia or in reduced renal function. Therefore, Delmuno should only be given to such patients after special considerations and after the doses of the individual components have been carefully titrated. Delmuno should only be given if the patient is in a stable circulatory condition (see section 4.3). In hypertensive patients without cardiac and renal insufficiency, hypotension may occur especially in patients with decreased
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